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TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines
We report herein an original and rapid synthesis of 2,3-diaryl N-tosylaziridines by TDAE strategy starting from ortho- or para-nitro(dichloromethyl)benzene derivatives and N-tosylimines. A mixture of cis/trans isomers was isolated from 1-(dichloromethyl)-4-nitrobenzene, whereas only trans-aziridines...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270596/ https://www.ncbi.nlm.nih.gov/pubmed/23884113 http://dx.doi.org/10.3390/molecules18077364 |
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author | Khoumeri, Omar Spitz, Cédric Terme, Thierry Vanelle, Patrice |
author_facet | Khoumeri, Omar Spitz, Cédric Terme, Thierry Vanelle, Patrice |
author_sort | Khoumeri, Omar |
collection | PubMed |
description | We report herein an original and rapid synthesis of 2,3-diaryl N-tosylaziridines by TDAE strategy starting from ortho- or para-nitro(dichloromethyl)benzene derivatives and N-tosylimines. A mixture of cis/trans isomers was isolated from 1-(dichloromethyl)-4-nitrobenzene, whereas only trans-aziridines were obtained from ortho-nitro derivatives. |
format | Online Article Text |
id | pubmed-6270596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62705962018-12-17 TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines Khoumeri, Omar Spitz, Cédric Terme, Thierry Vanelle, Patrice Molecules Communication We report herein an original and rapid synthesis of 2,3-diaryl N-tosylaziridines by TDAE strategy starting from ortho- or para-nitro(dichloromethyl)benzene derivatives and N-tosylimines. A mixture of cis/trans isomers was isolated from 1-(dichloromethyl)-4-nitrobenzene, whereas only trans-aziridines were obtained from ortho-nitro derivatives. MDPI 2013-06-24 /pmc/articles/PMC6270596/ /pubmed/23884113 http://dx.doi.org/10.3390/molecules18077364 Text en © 2013 by the authors. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Communication Khoumeri, Omar Spitz, Cédric Terme, Thierry Vanelle, Patrice TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines |
title | TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines |
title_full | TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines |
title_fullStr | TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines |
title_full_unstemmed | TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines |
title_short | TDAE Strategy for the Synthesis of 2,3-Diaryl N-Tosylaziridines |
title_sort | tdae strategy for the synthesis of 2,3-diaryl n-tosylaziridines |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270596/ https://www.ncbi.nlm.nih.gov/pubmed/23884113 http://dx.doi.org/10.3390/molecules18077364 |
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